Canonical Allele Identifier: CA348048188

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108897138T>A , CM000664.2:g.108897138T>A GRCh38
NC_000002.11:g.109513594T>A , CM000664.1:g.109513594T>A GRCh37
NC_000002.10:g.108880026T>A NCBI36
NG_008257.1:g.97235A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000258443.7:c.1116A>T (EDAR) MANE Select ENSP00000258443.2:p.Lys372Asn
ENST00000258443.6:c.1116A>T (EDAR) ENSP00000258443.2:p.Lys372Asn
ENST00000376651.1:c.1212A>T (EDAR) ENSP00000365839.1:p.Lys404Asn
ENST00000409271.5:c.1212A>T (EDAR) ENSP00000386371.1:p.Lys404Asn
NM_022336.3:c.1116A>T (EDAR) NP_071731.1:p.Lys372Asn
XM_006712204.1:c.1212A>T (EDAR) XP_006712267.1:p.Lys404Asn
XM_011510502.1:c.1263A>T (EDAR) XP_011508804.1:p.Lys421Asn
XM_011510503.1:c.1167A>T (EDAR) XP_011508805.1:p.Lys389Asn
XM_011510504.1:c.543A>T (EDAR) XP_011508806.1:p.Lys181Asn
XM_011510502.2:c.1356A>T (EDAR) XP_011508804.2:p.Lys452Asn
XM_011510503.2:c.1260A>T (EDAR) XP_011508805.2:p.Lys420Asn
XM_017004623.2:c.8370+124092T>A (RANBP2) XP_016860112.1:n.8370+124092T>A
NM_022336.4:c.1116A>T (EDAR) MANE Select NP_071731.1:p.Lys372Asn